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Sequence analysis of the CDKN1B gene in patients with premature ovarian failure reveals a novel mutation potentially related to the phenotype. [electronic resource] by
- Ojeda, Diego
- Lakhal, Besma
- Fonseca, Dora Janneth
- Braham, Rim
- Landolsi, Hanène
- Mateus, Heidi Eliana
- Restrepo, Carlos Martín
- Elghezal, Hatem
- Saâd, Ali
- Laissue, Paul
Producer: 20110826
In:
Fertility and sterility vol. 95
Availability: No items available.
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59640.
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